Lung reduction system

• US 7,896,008 B2
• Filed: 08/06/2007
• Issued: 03/01/2011
• Est. Priority Date: 06/03/2003
• Status: Expired due to Fees

• Current Assignee: Portaero, Inc
• Original Assignee: Portaero, Inc
• Inventors: Tanaka, Don
• Primary Examiner(s): Look; Edward
• Assistant Examiner(s): LOUIS, LATOYA M
• Application Number:
  US11/834,590
• Publication Number:
  US 20070270776A1
• Time in Patent Office: 1,303 Days
• Field of Search: 128/200.24, 128/200.26, 128/207.14, 128/207.15, 128/207.16, 623/9, 623/23.64, 623/23.65
• US Class Current: 128/207.16
• CPC Class Codes: A61F 2002/043 Bronchi
• CPC Class Codes: A61M 16/04 Tracheal tubes catheters in general A61M25/00
• CPC Class Codes: A61M 16/0406 implanted flow modifiers
• CPC Class Codes: A61M 16/101 using an oxygen concentrator
• CPC Class Codes: A61M 16/106 in a path
• CPC Class Codes: A61M 2202/0007 introduced into the body
• CPC Class Codes: A61M 2202/0208 Oxygen
• CPC Class Codes: A61M 2202/03 Gases in liquid phase, e.g. cryogenic liquids
• CPC Class Codes: A61M 2205/0244 Micromachined materials, e.g. made from silicon wafers, microelectromechanical systems [MEMS] or comprising nanotechnology
• CPC Class Codes: A61M 2210/1039 Lungs
• CPC Class Codes: A61M 39/0247 Semi-permanent or permanent transcutaneous or percutaneous access sites to the inside of the body peritoneal dialysis catheters A61M1/285; tracheostomy devices A61M16/0465; measuring pressure within the body A61B5/03; colostomy devices A61F5/445; gastrotomy feeding tubes A61J15/0015; means for fixing a feeding tube outside of the body A61J15/0053

Abstract

A lung-volume-reduction device for treating a lung to relieve symptoms of chronic obstructive pulmonary disease and/or emphysema. The device includes a chest-mounted housing and a conduit which projects from the housing through an aperture in the chest of the patient into the lung. The other end of the conduit is connected to flow-control device which may include a valve such as a one-way valve, check valve or pressure-actuated valve. The flow-control device is positioned within the chest-mounted housing. The lung-volume-reduction device permits gasses to pass through the conduit and flow-control device and vent to atmosphere external of the patient.

Claims

1. A method that uses a lung-volume-reduction device having a housing adapted to be secured to a chest of a patient, a conduit projecting from the housing, and a gas outlet positioned within the housing and in fluid communication with the conduit, wherein the method comprises:

(a) inserting the conduit through an aperture in the chest wall of the patient into the lung of the patient, wherein the aperture passes from external to the patient through skin of the chest wall, through a parietal membrane and through a visceral membrane into the lung, and wherein the visceral membrane is sealed to the parietal membrane around the aperture to prevent pneumothorax; and

(b) securing the housing to the chest of the patient external to the patient so that air within the lung may vent to atmosphere external to the patient through the conduit via the housing.

2. The method of claim 1, further comprising the steps of:

(c) removing at least a portion of the lung volume reduction device;

(d) disposing of said at least a portion of the lung volume reduction device; and

(e) replacing said at least a portion of the lung volume reduction device.

3. The method of claim 1, further comprising:

(c) removing at least a portion of the lung volume reduction device;

(d) disposing of said at least a portion of the lung volume reduction device;

(e) replacing said at least a portion of the lung volume reduction device; and

(f) repeating steps (c), (d) and (e) at regular intervals.

4. The method of claim 1, further comprising:

(c) removing at least a portion of the lung volume reduction device;

(d) disposing of said at least a portion of the lung volume reduction device;

(e) replacing said at least a portion of the lung volume reduction device; and

(f) repeating steps (c), (d) and (e) when needed to maintain cleanliness.

5. The method of claim 1, further comprising:

(c) permitting gas within the lung to vent to atmosphere external to the patient directly from the housing.

6. The method of claim 1, wherein step (b) comprises securing the conduit to the skin of the chest of the patient with a biocompatible adhesive.

7. A method for treating chronic obstructive pulmonary disease comprising:

(a) receiving a device having a housing adapted to be secured to a chest of a patient, a conduit projecting from the housing, and a gas outlet positioned within the housing and in fluid communication with the conduit;

(b) inserting the conduit through an aperture in the chest wall of the patient into the lung of the patient, wherein the aperture passes from external to the patient through skin of the chest wall, through a parietal membrane and through a visceral membrane into the lung, and wherein the visceral membrane is sealed to the parietal membrane around the aperture to prevent pneumothorax; and

(c) securing the housing to the chest of the patient external to the patient so that air within the lung may vent to atmosphere external to the patient through the conduit via the housing.

8. The method of claim 7, further comprising:

(d) permitting gas within the lung to vent to atmosphere external to the patient directly from the housing.

9. The method of claim 7, wherein step (b) comprises securing the conduit to the skin of the chest of the patient with a biocompatible adhesive.

10. The method of claim 7, wherein step (a) comprises receiving a self-contained device having a housing adapted to be secured to a chest of a patient, a conduit projecting from the housing, and a gas outlet positioned within the housing and in fluid communication with the conduit.

11. The method of claim 7 wherein step (a) comprises receiving a device having a housing adapted to be secured to a chest of a patient, a conduit projecting from the housing, and a gas outlet positioned within the housing and in fluid communication with the conduit, the device further comprising an expandable member connected to the conduit and adapted to secure the conduit within the lung of the patient.

12. The method of claim 7 wherein step (a) comprises receiving a device having a housing adapted to be secured to a chest of a patient, a conduit projecting from the housing, and a gas outlet positioned within the housing and in fluid communication with the conduit, the housing further comprising a planar surface bearing a biocompatible adhesive positioned to secure the housing to the chest of the patient.

13. The method of claim 7 wherein step (a) comprises receiving a device having a housing adapted to be secured to a chest of a patient, a conduit projecting from the housing, and a gas outlet positioned within the housing and in fluid communication with the conduit, wherein the gas outlet comprises a valve configured to prevent air external to the patient from entering the lung through the conduit.

14. The method of claim 7 wherein:

step (a) comprises receiving a device having a housing adapted to be secured to a chest of a patient, a conduit projecting from the housing, the housing having a biocompatible adhesive to secure the housing to the chest of the patient, and a gas outlet positioned within the housing and in fluid communication with the conduit; and

step (c) comprises securing the housing to the chest of the patient external to the patient with the biocompatible adhesive so that air within the lung may vent to atmosphere external to the patient through the conduit via the housing.

15. The method of claim 7, further comprising the steps of:

(d) removing at least a portion of the device;

(e) disposing of said at least a portion of the device; and

(f) replacing said at least a portion of the device.

16. The method of claim 7, further comprising:

(d) removing at least a portion of the device;

(e) disposing of said at least a portion of the device;

(f) replacing said at least a portion of the device; and

(g) repeating steps (d), (e) and (f) at regular intervals.

17. A method for treating chronic obstructive pulmonary disease comprising:

(a) receiving a device having an external component, the external component having a planar surface adapted to be secured to the chest of a patient, a conduit projecting from the planar surface of the external component, and a gas outlet positioned within the external component and in fluid communication with the conduit;

(b) inserting the conduit through an aperture in the chest wall of the patient into the lung of the patient, wherein the aperture passes from external to the patient through skin of the chest wall, through a parietal membrane and through a visceral membrane into the lung, and wherein the visceral membrane is sealed to the parietal membrane around the aperture to prevent pneumothorax; and

(c) securing the external component to the chest of the patient external to the patient so that air within the lung may vent to atmosphere external to the patient through the conduit via the external component.

18. The method of claim 17, further comprising:

(d) permitting gas within the lung to vent to atmosphere external to the patient directly from the external component.

19. The method of claim 17 wherein:

step (a) comprises receiving a device having an external component, the external component having a planar surface adapted to be secured to the chest of a patient, the planar surface having a biocompatible adhesive to secure the external component to the chest of the patient, a conduit projecting from the planar surface of the external component, and a gas outlet positioned within the external component and in fluid communication with the conduit; and

step (c) comprises securing the planar surface of the external component to the chest of the patient with the biocompatible adhesive external to the patient so that air within the lung may vent to atmosphere external to the patient through the conduit via the external component.

20. The method of claim 17, further comprising the steps of:

(d) removing at least a portion of the device;

(e) disposing of said at least a portion of the device; and

(f) replacing said at least a portion of the device.